ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.6915G>T (p.Glu2305Asp)

gnomAD frequency: 0.00001  dbSNP: rs778211562
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomics Program, Sidra Medicine RCV001293193 SCV001434191 likely benign Primary dilated cardiomyopathy criteria provided, single submitter research

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